A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126877



Internal ID20693917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159454287..159457680hg38UCSC Ensembl
chr5:158881295..158884688hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg383394
hg193394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403836
Supporting Variants
Samples
Known GenesLOC285627
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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